Membrane-bound O-acyltransferase involved in the remodeling of glycosylphosphatidylinositol (GPI) anchors. Related to fungal GUP1 proteins.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005737 | cytoplasm | 2 | 5 |
GO:0005783 | endoplasmic reticulum | 5 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
Related structures:
AlphaFold database: A4HA77
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016746 | acyltransferase activity | 3 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.358 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.349 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.602 |
DEG_SPOP_SBC_1 | 456 | 460 | PF00917 | 0.571 |
DEG_SPOP_SBC_1 | 46 | 50 | PF00917 | 0.618 |
DOC_CDC14_PxL_1 | 486 | 494 | PF14671 | 0.427 |
DOC_CYCLIN_yCln2_LP_2 | 42 | 45 | PF00134 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 434 | 440 | PF00134 | 0.441 |
DOC_PP1_RVXF_1 | 354 | 361 | PF00149 | 0.420 |
DOC_PP2B_LxvP_1 | 42 | 45 | PF13499 | 0.633 |
DOC_PP2B_LxvP_1 | 434 | 437 | PF13499 | 0.441 |
DOC_PP4_FxxP_1 | 264 | 267 | PF00568 | 0.326 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.256 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 173 | 181 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 206 | 211 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 345 | 351 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 356 | 361 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 455 | 463 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 464 | 470 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 475 | 484 | PF00244 | 0.213 |
LIG_Actin_WH2_2 | 341 | 358 | PF00022 | 0.411 |
LIG_BRCT_BRCA1_1 | 528 | 532 | PF00533 | 0.558 |
LIG_CtBP_PxDLS_1 | 541 | 545 | PF00389 | 0.568 |
LIG_deltaCOP1_diTrp_1 | 140 | 146 | PF00928 | 0.347 |
LIG_deltaCOP1_diTrp_1 | 556 | 561 | PF00928 | 0.571 |
LIG_eIF4E_1 | 100 | 106 | PF01652 | 0.271 |
LIG_eIF4E_1 | 429 | 435 | PF01652 | 0.441 |
LIG_eIF4E_1 | 477 | 483 | PF01652 | 0.241 |
LIG_EVH1_1 | 43 | 47 | PF00568 | 0.626 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.626 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.618 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.724 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.251 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.454 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.393 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.642 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.254 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.584 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.633 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.317 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.294 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.340 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.313 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.441 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.639 |
LIG_LIR_Apic_2 | 84 | 90 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 147 | 158 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 251 | 259 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 445 | 454 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 468 | 478 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 514 | 525 | PF02991 | 0.248 |
LIG_LIR_Gen_1 | 529 | 540 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 74 | 82 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 468 | 474 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.641 |
LIG_Pex14_1 | 316 | 320 | PF04695 | 0.455 |
LIG_Pex14_1 | 346 | 350 | PF04695 | 0.335 |
LIG_Pex14_2 | 166 | 170 | PF04695 | 0.291 |
LIG_Pex14_2 | 522 | 526 | PF04695 | 0.481 |
LIG_Pex14_2 | 557 | 561 | PF04695 | 0.603 |
LIG_PTB_Apo_2 | 107 | 114 | PF02174 | 0.266 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.371 |
LIG_SH2_CRK | 453 | 457 | PF00017 | 0.477 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.663 |
LIG_SH2_GRB2like | 135 | 138 | PF00017 | 0.310 |
LIG_SH2_NCK_1 | 75 | 79 | PF00017 | 0.663 |
LIG_SH2_STAP1 | 135 | 139 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 469 | 473 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.264 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.627 |
LIG_SH2_STAT3 | 315 | 318 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.324 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.370 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.669 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.264 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.427 |
LIG_SUMO_SIM_anti_2 | 479 | 485 | PF11976 | 0.241 |
LIG_SUMO_SIM_anti_2 | 93 | 99 | PF11976 | 0.214 |
LIG_SUMO_SIM_par_1 | 550 | 556 | PF11976 | 0.441 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.228 |
LIG_TRFH_1 | 432 | 436 | PF08558 | 0.441 |
LIG_TYR_ITIM | 451 | 456 | PF00017 | 0.480 |
LIG_TYR_ITIM | 515 | 520 | PF00017 | 0.441 |
LIG_UBA3_1 | 126 | 133 | PF00899 | 0.288 |
LIG_WRC_WIRS_1 | 105 | 110 | PF05994 | 0.335 |
LIG_WRC_WIRS_1 | 150 | 155 | PF05994 | 0.221 |
LIG_WRC_WIRS_1 | 244 | 249 | PF05994 | 0.223 |
LIG_WRC_WIRS_1 | 357 | 362 | PF05994 | 0.277 |
LIG_WRC_WIRS_1 | 444 | 449 | PF05994 | 0.487 |
LIG_WW_1 | 436 | 439 | PF00397 | 0.441 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.626 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.259 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.643 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.647 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.657 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.635 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.342 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.355 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.380 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.519 |
MOD_CMANNOS | 558 | 561 | PF00535 | 0.403 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.604 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.377 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.538 |
MOD_GlcNHglycan | 195 | 200 | PF01048 | 0.455 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.482 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.554 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.371 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.612 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.299 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.643 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.333 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.264 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.646 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.248 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.641 |
MOD_LATS_1 | 18 | 24 | PF00433 | 0.616 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.402 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.459 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.469 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.610 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.685 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.353 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.363 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.409 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.453 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.376 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.618 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.590 |
MOD_NEK2_2 | 346 | 351 | PF00069 | 0.260 |
MOD_NEK2_2 | 430 | 435 | PF00069 | 0.241 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.608 |
MOD_PK_1 | 81 | 87 | PF00069 | 0.561 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.381 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.631 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.351 |
MOD_PKB_1 | 204 | 212 | PF00069 | 0.609 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.606 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.262 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.365 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.348 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.228 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.643 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.241 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.368 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.407 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.358 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.244 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.446 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.441 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.249 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.668 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.682 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.663 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.628 |
TRG_DiLeu_BaEn_1 | 327 | 332 | PF01217 | 0.341 |
TRG_DiLeu_BaEn_2 | 505 | 511 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 353 | 358 | PF01217 | 0.398 |
TRG_DiLeu_LyEn_5 | 122 | 127 | PF01217 | 0.283 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.617 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 544 | 546 | PF00400 | 0.558 |
TRG_NES_CRM1_1 | 542 | 556 | PF08389 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2M9 | Leptomonas seymouri | 36% | 100% |
A0A3Q8IAC1 | Leishmania donovani | 62% | 72% |
A0A3Q8IBC3 | Leishmania donovani | 65% | 93% |
A0A3Q8IBE0 | Leishmania donovani | 56% | 67% |
A0A3Q8IDD7 | Leishmania donovani | 62% | 72% |
A0A3S5H769 | Leishmania donovani | 65% | 82% |
A0A3S7WVJ2 | Leishmania donovani | 57% | 67% |
A0A3S7WVK4 | Leishmania donovani | 64% | 72% |
A4HA75 | Leishmania braziliensis | 72% | 100% |
A4HA76 | Leishmania braziliensis | 73% | 100% |
A4HA81 | Leishmania braziliensis | 96% | 86% |
A4HA82 | Leishmania braziliensis | 98% | 75% |
A4HA83 | Leishmania braziliensis | 50% | 100% |
E9AGT0 | Leishmania infantum | 57% | 67% |
E9AGT1 | Leishmania infantum | 66% | 98% |
E9AGT2 | Leishmania infantum | 65% | 100% |
E9AGT3 | Leishmania infantum | 64% | 72% |
E9AGT4 | Leishmania infantum | 62% | 72% |
E9AS85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 73% |
E9AS86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4QD78 | Leishmania major | 64% | 100% |
Q4QD79 | Leishmania major | 64% | 100% |
Q4QD80 | Leishmania major | 67% | 100% |
Q4QD81 | Leishmania major | 61% | 100% |
Q4QD82 | Leishmania major | 75% | 100% |